Phytochemical investigation of the underground parts of Agapanthus inapertus (Liliaceae) has resulted in the isolation of three new spirostanol glycosides (1, 3, and 4), along with a known spirostanol glycoside (2) and two known spirostanols (5 and 6). The structures of the new glycosides were determined by spectroscopic analysis and the results of hydrolytic cleavage. The isolated compounds were evaluated for their cytotoxic activity against HL-60 human promyelocytic leukemia cells.
SavchenkoT, WhitingP, SarkerSD, DinanL. (1997) Phytoecdysteroids in genus Agapanthus (Alliaceae). Biochemical Systematics and Ecology, 25, 623–629.
2.
NakamuraO, MimakiY, SashidaY, NikaidoT, OhmotoT. (1993) Agapanthussaponins A–D, new potent cAMP phosphodiesterase inhibitors from the underground parts of Agapanthus inapertus. Chemical & Pharmaceutical Bulletin, 41, 1784–1789.
3.
MimakiY, YokosukaA, KurodaM, SashidaY. (2001) Cytotoxic activities and structure–cytotoxic relationships of steroidal saponins. Biological & Pharmaceutical Bulletin, 24, 1286–1289.
4.
BarileE, ZolfaghariB, SajjadiE, LanzottiV. (2004) Saponins from Allium elbuzanse. Journal of Natural Products, 67, 2037–2042.
5.
GonzalezAG, FreireR, FranciscoCG, SalazarJA, SuarezE. (1974) 7-Dehydroagapanthagenin and 8(14)-dehydroagapanthagenin, two new spirostan sapogenins from Agapanthus africanus. Phytochemistry, 13, 627–632.
6.
StephenT. (1956) Saponins and sapogenins. IV. Agapanthagenin (22a-spirostan-2α:3β:5α-triol), a new sapogenin from Agapanthus species. Journal of the Chemical Society, 1167–1169.
7.
AgrawalPK, JainDC, GuptaRK, ThakurRS. (1985) Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins. Phytochemistry, 24, 2479–2496.
8.
SargentJM, TaylorCG. (1989) Appraisal of the MTT assay as a rapid test of chemosensitivity in acute myeloid leukemia. British Journal of Cancer, 60, 206–210.